Caputo Lisa M, Jensen Judd, Whaley Michelle, Kozlowski Mark J, Fanale Christopher V, Wagner Jeffrey C, Orlando Alessandro, Bar-Or David
Department of Trauma and Stroke Research, Swedish Medical Center, Englewood, CO, USA.
Department of Neurology, Swedish Medical Center, Englewood, CO, USA.
Neurohospitalist. 2017 Apr;7(2):70-73. doi: 10.1177/1941874416672783. Epub 2016 Oct 21.
The safety and efficacy of intravenous tissue plasminogen activator (IV tPA) following acute ischemic stroke (AIS) is dependent on its timely administration. In 2014, our Comprehensive Stroke Center designed and implemented a computed tomography-Direct protocol to streamline the evaluation process of suspected patients with AIS, with the aim of reducing door-to-needle (DTN) times. The objectives of our study were to describe the protocol development and implementation process, and to compare DTN times and symptomatic intracranial hemorrhage (sICH) rates before and after protocol implementation.
Data were prospectively collected for patients with AIS receiving IV tPA between January 1, 2010, and May 31, 2015. The DTN times, examined as median times and time treatment windows, and sICH rates were compared pre- and postimplementation.
Two hundred ninety-five patients were included in the study. After protocol implementation, median DTN times were significantly reduced (38 vs 28 minutes; < .001). The distribution of patients treated in the three time treatment windows described below changed significantly, with an increase in patients with DTN times of 30 minutes or less, and a decrease in patients with DTN times 31 to 60 minutes and over 60 minutes ( < .001). There were two cases of sICH prior to implementation and one sICH case postimplementation.
The implementation of a protocol that streamlined the processing of suspected patients with AIS significantly reduced DTN time without negatively impacting patient safety.
急性缺血性卒中(AIS)后静脉注射组织型纤溶酶原激活剂(IV tPA)的安全性和有效性取决于其及时给药。2014年,我们的综合卒中中心设计并实施了一项计算机断层扫描直接方案,以简化疑似AIS患者的评估流程,目的是缩短门到针(DTN)时间。我们研究的目的是描述该方案的制定和实施过程,并比较方案实施前后的DTN时间和症状性颅内出血(sICH)发生率。
前瞻性收集2010年1月1日至2015年5月31日期间接受IV tPA治疗的AIS患者的数据。比较实施前后的DTN时间(以中位数时间和治疗时间窗表示)和sICH发生率。
295例患者纳入研究。方案实施后,DTN中位数时间显著缩短(38分钟对28分钟;P<0.001)。在以下描述的三个治疗时间窗内接受治疗的患者分布发生了显著变化,DTN时间在30分钟及以内的患者增加,DTN时间在31至60分钟以及超过60分钟的患者减少(P<0.001)。实施前有2例sICH,实施后有1例sICH。
实施一项简化疑似AIS患者处理流程的方案显著缩短了DTN时间,且未对患者安全产生负面影响。